Test Directory
| Test Code | |||
| HPVMD | |||
| Test Name | |||
| Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by PCR | |||
| CPT Codes | |||
| 87626 | |||
| Expected Turnaround Time | |||
| 1 - 3 days | |||
| Clinical Utility | |||
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Indicated for use for routine cervical cancer screening as per professional medical guidelines, including triage of ASC-US cytology, co-testing with cytology, and HPV primary screening of women to assess the risk for cervical precancer and cancer. Patients should be followed-up in accordance with professional medical guidelines, results from prior screening, medical history, and other risk factors. This test detects the high-risk HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68. |
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| Specimen and Container Info | |||
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Specimen Type: Cervical specimens collected in PreservCyt Solution Collection Container: Thin Prep Vial Desired Specimen Volume: 10 mL Minimum Acceptable Volume: 3 mL |
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| Collection Instructions | |||
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| Transport Instructions | |||
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Transport to the laboratory at room temperature. |
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| Stability Requirements | |||
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| Causes for Rejection | |||
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| Methodology | |||
| Polymerase Chain Reaction (PCR) | |||
| Reference Intervals | |||
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HPV Virus Not Detected |
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| Limitations | |||
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This test detects the high-risk HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68. |
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| Performing Location | |||
| Roble Road Core Laboratory | |||
| Alternate Names | |||
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| Testing Schedule | |||
| Routine, Monday - Friday no holidays | |||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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